XEN 63 Glaucoma Treatment System - EUDAMED Registration 05016007207583

Access comprehensive regulatory information for XEN 63 Glaucoma Treatment System in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 05016007207583 and manufactured by Allergan Sales, LLC in United States.

This page provides complete registration details including trade name (XEN 63 GLAUCOMA TREATMENT SYSTEM), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.